Skip to content

A Study Comparing the Effects of Triamcinolone Injections and Platelet-Rich Plasma Therapy on Mouth Opening in Patients with Oral Submucous Fibrosis

Comparative evaluation of Triamcinolone versus Autologous Platelet Rich Plasma injection for management of Oral Submucous Fibrosis -A Prospective Study - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109148
Enrollment
30
Registered
2026-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K135- Oral submucous fibrosis

Interventions

Intervention1: Triamcinolone injection: intralesional injection of Triamcinolone acetonide 40mg/ml 1 ml per session, once weekly for 6 weeks in oral mucosa intralesional with standard physiotherapy

Sponsors

Hitkarini Dental College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients clinically diagnosed with Oral Submucous Fibrosis Classified under GROUP I GROUP III according to Ranganathan K et al (2001) Patients with reduced mouth opening and burning sensation in mouth.

Exclusion criteria

Exclusion criteria: Pregnant or lactating women . Patients who have any drug allergy. Patients showing signs of inflammatory reaction after injection. Patients with bleeding disorders. Medically compromised patients. Patients with clinical signs and symptoms or proven report of malignancy in oral cavity. Patients with Temporomandibular joint disorders or trauma to

Design outcomes

Primary

MeasureTime frame
change in interincisal mouth opening in millimetersTimepoint: baseline ( pre treatment), at the end of 6 months and at 3 months follow up

Secondary

MeasureTime frame
Reduction in burning sensation (measured by visual analog scale)Timepoint: baseline ( pre treatment), at the end of 6 months and at 3 months follow up;cheek flexibilityTimepoint: baseline ( pre treatment), at the end of 6 months and at 3 months follow up;change in color of tissue ( clinical)Timepoint: baseline ( pre treatment), at the end of 6 months and at 3 months follow up

Countries

India

Contacts

Public ContactVipul Ughade

Hitkarini Dental College and Hospital

vipul.ughade@gmail.com8717875443

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026